A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188856



Internal ID20755896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55835501..55842400hg38UCSC Ensembl
chr14:56302219..56309118hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188856
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer